PRO-LIANCE CORE Learning
Clinical Evaluation
This 4h PRO-LIANCE Core Learning provides a practical introduction to Clinical Evaluation under the MDR. Participants learn the key requirements, understand the role of CEP and CER, identify common evidence gaps, and explore the interfaces with Risk Management, PMS, PMCF, and technical documentation.
Through expert insights, interactive exercises, and practical examples, participants gain a clear understanding of what matters most in Clinical Evaluation and where further action may be needed.
PRICING AND REGISTRATION
Choose your spot
- NORMAL PRICE
Standard registration fee: 490.00 € excl. VAT - EARLY BIRD FEE
Register 8 weeks prior to event and profit from our early bird fee (440.00 €/person excl. VAT)! - SPECIAL OFFER FOR COMPANIES
Special offer for companys registering more than two participants (440.00 €/person excl. VAT) per company!
What we will cover
Learn from Florian Tolkmitt, one of the most known voices regarding Clinical Evaluation of Medical Devices.
- What really matters in Clinical Evaluation under the MDR
- How the main documents and processes fit together
- Where typical weaknesses in CEP, CER, literature search, equivalence, and PMCF arise
- Which are the next steps relevant for your devices or processes
- Which topics require deeper practical training
Speaker
Regulatory & Clinical Evaluation Expert
PRO-LIANCE GLOBAL SOLUTIONS GmbH, Managing Director
Florian Tolkmitt is Co-Founder & Managing Director of PRO-LIANCE GLOBAL SOLUTIONS GmbH. He is passionate about Clinical Evaluation of Medical Devices, driving innovation and excellence to ensure the highest standards and safer patient outcomes.
Additional information:
- Registration and event will be managed via Microsoft Teams. Billing and cancellation information will be sent to you via a separate email after registration.
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